Yarullina Liubov, Kalatskaja Joanna, Tsvetkov Vyacheslav, Burkhanova Guzel, Yalouskaya Ninel, Rybinskaya Katerina, Zaikina Evgenia, Cherepanova Ekaterina, Hileuskaya Kseniya, Nikalaichuk Viktoryia
Institute of Biochemistry and Genetics, pr. Oktyabrya, 71, 450054 Ufa, Russia.
Institute of Experimental Botany Named after V.F. Kuprevich, ul. Akademicheskaya, 27, 220072 Minsk, Belarus.
Plants (Basel). 2024 Aug 9;13(16):2210. doi: 10.3390/plants13162210.
Viral diseases of potatoes are among the main problems causing deterioration in the quality of tubers and loss of yield. The growth and development of potato plants largely depend on soil moisture. Prevention strategies require comprehensive protection against pathogens and abiotic stresses, including modeling the beneficial microbiome of agroecosystems combining microorganisms and immunostimulants. Chitosan and its derivatives have great potential for use in agricultural engineering due to their ability to induce plant immune responses. The effect of chitosan conjugate with caffeic acid (ChCA) in combination with 47 on the transcriptional activity of PR protein genes and changes in the proteome of potato plants during potato virus Y (PVY) infection and drought was studied. The mechanisms of increasing the resistance of potato plants to PVY and lack of moisture are associated with the activation of transcription of genes encoding PR proteins: the main protective protein (PR-1), chitinase (PR-3), thaumatin-like protein (PR-5), protease inhibitor (PR-6), peroxidase (PR-9), and ribonuclease (PR-10), as well as qualitative and quantitative changes in the plant proteome. The revealed activation of the expression of marker genes of systemic acquired resistance and induced systemic resistance under the influence of combined treatment with and chitosan conjugate indicate that, in potato plants, the formation of resistance to viral infection in drought conditions proceeds synergistically. By two-dimensional electrophoresis of leaf proteins followed by MALDI-TOF analysis, 10 proteins were identified, the content and composition of which differed depending on the experiment variant. In infected plants treated with ChCA, the synthesis of proteinaceous RNase P 1 and oxygen-evolving enhancer protein 2 was enhanced in conditions of normal humidity, and 20 kDa chaperonin and TMV resistance protein N-like was enhanced in conditions of lack of moisture. The virus coat proteins were detected, which intensively accumulated in the leaves of plants infected with potato Y-virus. ChCA treatment reduced the content of these proteins in the leaves, and in plants treated with ChCA in combination with , viral proteins were not detected at all, both in conditions of normal humidity and lack of moisture, which suggests the promising use of chitosan derivatives in combination with bacteria in the regulation of plant resistance.
马铃薯病毒病是导致块茎品质下降和产量损失的主要问题之一。马铃薯植株的生长和发育很大程度上依赖于土壤湿度。预防策略需要对病原体和非生物胁迫进行全面防护,包括对结合微生物和免疫刺激剂的农业生态系统有益微生物群落进行建模。壳聚糖及其衍生物因其能够诱导植物免疫反应而在农业工程中具有巨大的应用潜力。研究了咖啡酸壳聚糖共轭物(ChCA)与47组合对马铃薯Y病毒(PVY)感染和干旱期间马铃薯植株PR蛋白基因转录活性及蛋白质组变化的影响。马铃薯植株对PVY和水分缺乏抗性增强的机制与编码PR蛋白的基因转录激活有关:主要保护蛋白(PR-1)、几丁质酶(PR-3)、类甜蛋白(PR-5)、蛋白酶抑制剂(PR-6)、过氧化物酶(PR-9)和核糖核酸酶(PR-10),以及植物蛋白质组的定性和定量变化。在与和壳聚糖共轭物联合处理的影响下,系统获得性抗性和诱导系统抗性标记基因表达的激活表明,在马铃薯植株中,干旱条件下对病毒感染抗性的形成是协同进行的。通过对叶片蛋白质进行二维电泳,随后进行MALDI-TOF分析,鉴定出10种蛋白质,其含量和组成因实验变体而异。在用ChCA处理的受感染植株中,正常湿度条件下蛋白质核糖核酸酶P 1和放氧增强蛋白2的合成增强,水分缺乏条件下20 kDa伴侣蛋白和烟草花叶病毒抗性蛋白N样蛋白的合成增强。检测到病毒外壳蛋白,其在感染马铃薯Y病毒的植株叶片中大量积累。ChCA处理降低了叶片中这些蛋白的含量,在用ChCA与组合处理的植株中,无论是正常湿度还是水分缺乏条件下,均未检测到病毒蛋白,这表明壳聚糖衍生物与细菌组合在调节植物抗性方面具有广阔的应用前景。